LD2H
遗传性耳聋综合征
Syndromic genetic deafness
- 上级条目
- 多发性发育异常或综合征
- 层级
- 3 级
跨章引用 同一概念在其他章节另有编码
- CATCH 22表型LD44.N0
- Pendred综合征5A00.02
- 全身性甲状腺激素抵抗5A05
- CHARGE综合征5A61.0
- 耳聋-视神经萎缩-痴呆5C53.2Y
- 外胚层发育不良-感音神经性聋LD27.0Y
- 甲状旁腺功能减退-聋-肾病LD27.0Y
- 肾小管酸中毒-聋GB90.44
- 镫骨强直伴拇指和趾扁宽LD2F.1Y
- Stickler综合征LD2F.1Y
- 硫胺素反应性巨幼红细胞性贫血综合征5C63.Y
- 线粒体性脑病，伴乳酸性酸中毒和中风样发作8C73.Y
- Norrie病LD21.Y
- Fechtner综合征3B64.01
- 脊椎骨骺发育不良，MacDermot型LD24.3
- 口-面-指（趾）综合征1型LD25.00
- 口-面-指（趾）综合征2型LD25.00
- 口-面-指（趾）综合征3型LD25.00
- 口-面-指（趾）综合征4型LD25.00
- 口-面-指（趾）综合征6型LD25.00
- 口-面-指（趾）综合征8型LD25.00
- 耳腭指[趾]综合征LD25.1
- Kearns-Sayre综合征9C82.0
- 多发性骨性连接综合征LD26.3
- 关节挛缩样手畸形-感音神经性耳聋LD26.4Y
- Cockayne综合征LD2B
- 角膜炎-鱼鳞病-耳聋综合征LD27.2
- 缝隙连接蛋白掌跖角皮病伴感音神经性耳聋EC20.30
- 耳聋–釉质发育不全-甲缺损LD27.0Y
- TIETZ色素减少症-耳聋综合征EC23.2Y
- LEOPARD综合征LD2F.1Y
- 回状头皮-视网膜色素变性-感音神经性聋LD27.Y
- 耳聋-淋巴水肿-白血病综合征BD93.0
- 长QT综合征伴听力受损BC65.0
- 婴儿Bartter综合征伴聋GB90.43
英文词条（35）
- CATCH 22 phenotypeLD44.N0
- Pendred syndrome5A00.02
- Generalised resistance to thyroid hormone5A05
- CHARGE syndrome5A61.0
- Deafness - opticoacoustic nerve atrophy - dementia5C53.2Y
- Ectodermal dysplasia - sensorineural deafnessLD27.0Y
- Hypoparathyroidism - deafness - renal diseaseLD27.0Y
- Renal tubular acidosis - deafnessGB90.44
- Stapes ankylosis with broad thumbs and toesLD2F.1Y
- Stickler syndromeLD2F.1Y
- Thiamine-responsive megaloblastic anaemia syndrome5C63.Y
- Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes8C73.Y
- Norrie diseaseLD21.Y
- Fechtner syndrome3B64.01
- Spondyloepiphyseal dysplasia, MacDermot typeLD24.3
- Oral-facial-digital syndrome type 1LD25.00
- Oral-facial-digital syndrome type 2LD25.00
- Oral-facial-digital syndrome type 3LD25.00
- Oral-facial-digital syndrome type 4LD25.00
- Oral-facial-digital syndrome type 6LD25.00
- Oral-facial-digital syndrome type 8LD25.00
- Otopalatodigital syndromeLD25.1
- Kearns-Sayre syndrome9C82.0
- Multiple synostoses syndromeLD26.3
- Arthrogryposis-like hand anomaly - sensorineural deafnessLD26.4Y
- Cockayne syndromeLD2B
- Keratitis – ichthyosis – deafness syndromeLD27.2
- Connexin palmoplantar keratoderma with sensorineural deafnessEC20.30
- Deafness – enamel hypoplasia – nail defectsLD27.0Y
- Tietz hypomelanosis – deafness syndromeEC23.2Y
- LEOPARD syndromeLD2F.1Y
- Cutis verticis gyrata - retinitis pigmentosa - sensorineural deafnessLD27.Y
- Deafness, lymphoedema and leukaemia syndromeBD93.0
- Long QT syndrome with hearing impairmentBC65.0
- Infantile Bartter syndrome with deafnessGB90.43
子条目 共 7 条
后组配轴 Postcoordination
该条目未定义后组配轴，直接使用上面的编码即可。后组配是在主干编码之后追加侧别、具体解剖部位、严重程度、病因等细节的可选组合方式，不是必填项。